Influence of the glutathione s-transferase gene polymorphisms on the susceptibility to basal cell skin carcinoma

Rev Med Chil. 2007 Mar;135(3):301-6. doi: 10.4067/s0034-98872007000300004. Epub 2007 Apr 26.

Abstract

Background: The identification of groups at high risk is fundamental to determine preventive strategies for skin cancer. Destructive reactive oxygen species produced by UVA or chemical carcinogens are metabolized by a series of enzymes. Polymorphisms of genes encoding for these enzymes may produce defective proteins with a diminished ability to detoxify a wide range of carcinogens.

Aims: To ascertain the influence and potential interactions of several polymorphisms of genes encoding four important antioxidant GST enzymes in the susceptibility to cancer among Brazilians.

Material and methods: We compared the genotypes of Glutathione S-Transferase mu, theta, pi and omega (GSTM1, GSTT1, GSTP1 and GSTO2) in a group of 102 patients with skin lesions and 124 controls.

Results: Patients with Basal Cell Skin Carcinoma (BCC) presented the combined GSTM1-GSTT1+ genotype more frequently (49.1%) than controls (29.8%) (Fisher test; p=0.04), conferring a 2.273 (Odds Ratio; 95% CI=1.199-4.308) higher risk for BCC. We were not able to find any other association between genotypes or between any genotype and the patients' clinical features.

Conclusions: The GST profile may help identify Brazilian individuals at higher risk for BCC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Carcinoma, Basal Cell / enzymology
  • Carcinoma, Basal Cell / genetics*
  • Epidemiologic Methods
  • Female
  • Genetic Predisposition to Disease / genetics*
  • Genotype
  • Glutathione S-Transferase pi / genetics
  • Glutathione Transferase / genetics*
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Genetic / genetics*
  • Polymorphism, Restriction Fragment Length
  • Reactive Oxygen Species / metabolism
  • Skin Neoplasms / enzymology
  • Skin Neoplasms / genetics*

Substances

  • Reactive Oxygen Species
  • glutathione S-transferase T1
  • GSTO2 protein, human
  • Glutathione S-Transferase pi
  • Glutathione Transferase
  • glutathione S-transferase M1